Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519743 | 0.827 | 0.120 | Y | 1196852 | missense variant | A/C | snv | 6 | |||
rs17069665 | 0.882 | 0.120 | 6 | 108620265 | intron variant | A/C;G | snv | 4 | |||
rs9400241 | 0.882 | 0.120 | 6 | 108682786 | 3 prime UTR variant | C/A;G | snv | 4 |